Unprecedented cholestane analogs have been synthesized by Diels-Alder reactions between a diene generated in high yields from vitamin D3 and appropriate dienophiles. This strategy is useful for the scarcely utilized A+CD → ABCD approach to the tetracyclic steroid nucleus.
Synthesis of unusual cholestane analogs by Diels-Alder reaction (A+CD –> ABCD).
DE RICCARDIS, Francesco;IZZO, Irene;TEDESCO, Consiglia;SODANO, Guido
1997
Abstract
Unprecedented cholestane analogs have been synthesized by Diels-Alder reactions between a diene generated in high yields from vitamin D3 and appropriate dienophiles. This strategy is useful for the scarcely utilized A+CD → ABCD approach to the tetracyclic steroid nucleus.File in questo prodotto:
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